
pmid: 21221781
The transcription factor Juxtaposed with another zinc finger gene 1 (JAZF1) is a zinc finger protein that binds to the nuclear orphan receptor TR4. Recent evidence indicates that TR4 receptor functions as both a positive and negative regulator of transcription, but the role of JAZF1 in transcriptional mechanisms has not been elucidated. Recently, the incidence rate of congenital heart malformations was reported to be significantly elevated in patients who had neurofibromatosis 1 (NF1) with chromosomal microdeletion syndrome. Furthermore, Joined to JAZF1 (SUZ12) is expressed at high levels in the hearts of adult patients with NF1 microdeletion syndrome. Therefore, we hypothesized that ectopic expression of JAZF1 may lead to cardiac malformations that deleteriously affect the survival of neonates and adults. We sought to elucidate the role of JAZF1 in cardiac development using a Jazf1-overexpressing (Jazf1-Tg) mouse model. In Jazf1-Tg mice, Jazf1 mRNA expression was significantly elevated in the heart. Jazf1-Tg mice also showed cardiac defects, such as high blood pressure, electrocardiogram abnormalities, apoptosis of cardiomyocytes, ventricular non-compaction, and mitochondrial defects. In addition, we found that the expression levels of pro-apoptotic genes were elevated in the hearts of Jazf1-Tg mice. These findings suggest that Jazf1 overexpression may induce heart failure symptoms through the upregulation of pro-apoptotic genes in cardiomyocytes.
Heart Defects, Congenital, Heart Failure, Polycomb Repressive Complex 2, Gene Expression Regulation, Developmental, Nuclear Proteins, Blood Pressure, Heart, Mice, Transgenic, DNA-Binding Proteins, Repressor Proteins, Disease Models, Animal, Electrocardiography, Mice, Animals, RNA, Messenger, Apoptosis Regulatory Proteins, Carrier Proteins, Co-Repressor Proteins
Heart Defects, Congenital, Heart Failure, Polycomb Repressive Complex 2, Gene Expression Regulation, Developmental, Nuclear Proteins, Blood Pressure, Heart, Mice, Transgenic, DNA-Binding Proteins, Repressor Proteins, Disease Models, Animal, Electrocardiography, Mice, Animals, RNA, Messenger, Apoptosis Regulatory Proteins, Carrier Proteins, Co-Repressor Proteins
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